{
  "id": 18628,
  "label": "Marie Unna hereditary hypotrichosis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018631",
  "properties": {
    "xrefs": [
      "GARD:0003390",
      "MEDGEN:419706",
      "MESH:C535912",
      "Orphanet:444",
      "UMLS:C2931059"
    ],
    "synonyms": [
      "HR hypotrichosis",
      "MUHH",
      "Marie Unna congenital hypotrichosis",
      "hypotrichosis caused by mutation in HR",
      "hypotrichosis, Marie Unna type"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "A rare autosomal dominant hair loss disorder characterized by the absence or scarcity of scalp hair, eyebrows, and eyelashes at birth; coarse and wiry hair during childhood; and progressive hair loss beginning around puberty."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 5030,
      "label": "hypotrichosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4924,
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:4535",
          "ICD9:704.09",
          "MEDGEN:6993",
          "MESH:D007039",
          "NCIT:C34720",
          "OMIMPS:605389",
          "SCTID:53602002",
          "UMLS:C0020678"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A congenital condition, usually due to genetic aberrations, that is characterized by a lack of hair growth on the head and/or body."
      },
      "child_count": 38,
      "reference_id": "MONDO:0003037"
    }
  ],
  "children": [
    {
      "id": 14056,
      "label": "hypotrichosis 5",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18628
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110702",
          "GARD:0015585",
          "MEDGEN:440568",
          "MESH:C567554",
          "OMIM:612841",
          "UMLS:C2748535"
        ],
        "synonyms": [
          "HYPT5",
          "MUHH2",
          "Marie Unna hereditary hypotrichosis 2",
          "Muhh2",
          "hypotrichosis 5",
          "hypotrichosis type 5",
          "hypt5"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A hypotrichosis that has material basis in a mutation on chromosome 1p21.1-q21.3."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013017"
    },
    {
      "id": 24247,
      "label": "hypotrichosis 4",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18628
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110701",
          "GARD:0015078",
          "MEDGEN:413053",
          "MESH:C567718",
          "OMIM:146550",
          "UMLS:C2750815"
        ],
        "synonyms": [
          "HYPT4",
          "MUHH1",
          "Marie Unna hereditary hypotrichosis 1",
          "hypotrichosis 4",
          "hypotrichosis type 4",
          "hypotrichosis, Marie Unna type, 1"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0100522"
    }
  ],
  "roots": [
    {
      "id": 5030,
      "label": "hypotrichosis"
    }
  ]
}